Variant report

Variant	nsv1061772
Chromosome Location	chr19:43652661-43846382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3021)
CpG islands
(count:1283)
Chromatin interactive
region (count:17)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3021 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:43733581-43733686	K562	blood:	n/a	n/a
2	ATF1	chr19:43779068-43779071	K562	blood:	n/a	n/a
3	ATF3	chr19:43686016-43686763	A549	lung:	n/a	n/a
4	BACH1	chr19:43820857-43821149	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr19:43822401-43822627	K562	blood:	n/a	n/a
6	BACH1	chr19:43822387-43822697	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
8	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
9	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
10	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
11	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
12	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
13	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
15	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
16	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
17	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
18	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
20	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
23	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
24	CEBPB	chr19:43822954-43823273	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr19:43834287-43834297	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:43656349-43656822	Hela-S3	cervix:	n/a	chr19:43656521-43656532
27	CEBPB	chr19:43676596-43676779	K562	blood:	n/a	n/a
28	CEBPB	chr19:43768999-43769727	IMR90	lung:	n/a	n/a
29	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr19:43656430-43656683	A549	lung:	n/a	chr19:43656521-43656532
31	CEBPB	chr19:43705107-43705824	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr19:43656448-43656689	HepG2	liver:	n/a	chr19:43656521-43656532
33	CEBPB	chr19:43846192-43846480	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr19:43839550-43839831	HepG2	liver:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
35	CEBPB	chr19:43675341-43675474	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr19:43846212-43846413	A549	lung:	n/a	n/a
37	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
38	CEBPB	chr19:43668229-43668245	IMR90	lung:	n/a	n/a
39	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:43709791-43709942	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:43820878-43821315	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr19:43656390-43656701	K562	blood:	n/a	chr19:43656521-43656532
44	CEBPB	chr19:43686079-43686251	A549	lung:	n/a	n/a
45	CEBPB	chr19:43705598-43705699	IMR90	lung:	n/a	n/a
46	CEBPB	chr19:43653804-43654163	IMR90	lung:	n/a	n/a
47	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr19:43686010-43686301	A549	lung:	n/a	n/a
49	CEBPB	chr19:43759754-43759856	K562	blood:	n/a	n/a
50	CEBPB	chr19:43685962-43686735	A549	lung:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43774820-43774870	LNCaP	prostate:	n/a
2	chr19:43691930-43691980	A549	lung:	n/a
3	chr19:43774820-43774870	LNCaP	prostate:	n/a
4	chr19:43691930-43691980	A549	lung:	n/a
5	chr19:43774893-43774943	HRPEpiC	eye:	n/a
6	chr19:43709360-43709410	K562	blood:	n/a
7	chr19:43697480-43697530	Jurkat	blood:	n/a
8	chr19:43774893-43774943	CMK	blood:	n/a
9	chr19:43673501-43673551	HCT-116	colon:	n/a
10	chr19:43709832-43709882	AG04449	skin:	fetal
11	chr19:43680072-43680122	HCT-116	colon:	n/a
12	chr19:43691878-43691928	HL-60	blood:	n/a
13	chr19:43690996-43691046	SK-N-MC	brain:	n/a
14	chr19:43711249-43711299	SAEC	small airway:	n/a
15	chr19:43710277-43710327	BE2_C	brain:	n/a
16	chr19:43773649-43773699	SK-N-SH_RA	brain:	n/a
17	chr19:43680072-43680122	GM12891	blood:	n/a
18	chr19:43691878-43691928	SK-N-MC	brain:	n/a
19	chr19:43773649-43773699	HepG2	liver:	n/a
20	chr19:43711249-43711299	ECC-1	luminal epithelium:	n/a
21	chr19:43774820-43774870	HCF	heart:	n/a
22	chr19:43711064-43711114	HepG2	liver:	n/a
23	chr19:43774982-43775032	GM12878	blood:	n/a
24	chr19:43711064-43711114	HPAEpiC	pulmonary alveolar:	n/a
25	chr19:43711064-43711114	HUVEC	blood vessel:	n/a
26	chr19:43690622-43690672	AG09309	skin:	n/a
27	chr19:43774982-43775032	Caco-2	colon:	n/a
28	chr19:43709832-43709882	MCF10A-Er-Src	breast:	n/a
29	chr19:43711249-43711299	HMEC	breast:	n/a
30	chr19:43773649-43773699	AoSMC	blood vessel:	n/a
31	chr19:43697480-43697530	HMEC	breast:	n/a
32	chr19:43690996-43691046	NH-A	brain:	n/a
33	chr19:43774921-43774971	GM19239	blood:	n/a
34	chr19:43690622-43690672	GM19239	blood:	n/a
35	chr19:43691878-43691928	A549	lung:	n/a
36	chr19:43690996-43691046	HCM	heart:	n/a
37	chr19:43709754-43709804	NHBE	bronchial:	n/a
38	chr19:43774921-43774971	AG09309	skin:	n/a
39	chr19:43710277-43710327	AG10803	skin:	n/a
40	chr19:43774982-43775032	HCM	heart:	n/a
41	chr19:43709360-43709410	GM06990	blood:	n/a
42	chr19:43711249-43711299	PrEC	prostate:	n/a
43	chr19:43709832-43709882	IMR90	lung:	fetal
44	chr19:43691878-43691928	PFSK-1	brain:	n/a
45	chr19:43769725-43769775	HCF	heart:	n/a
46	chr19:43690996-43691046	GM12891	blood:	n/a
47	chr19:43711064-43711114	PrEC	prostate:	n/a
48	chr19:43691878-43691928	U87	brain:	n/a
49	chr19:43774893-43774943	HRE	kidney:	n/a
50	chr19:43774921-43774971	HCM	heart:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
2	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:
3	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:
4	chr19:43837425..43840449-chr19:43845958..43849291,3	MCF-7	breast:
5	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
6	chr19:43821071..43821590-chr19:43929652..43930334,2	MCF-7	breast:
7	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:
8	chr19:43820685..43821690-chr19:43929045..43930443,5	MCF-7	breast:
9	chr19:43835562..43838441-chr19:43843809..43845441,2	MCF-7	breast:
10	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
11	chr1:117602243..117602763-chr19:43822533..43823090,2	Hela-S3	cervix:
12	chr19:43837425..43840449-chr19:43845958..43849291,3	MCF-7	breast:
13	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
14	chr19:43820533..43821452-chr19:44166758..44167329,2	K562	blood:
15	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
16	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
17	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG4-3	chr19:43671924-43672287	NONHSAT066585
2	lnc-PSG4-2	chr19:43688934-43689087	NONHSAT066587
3	lnc-PSG4-2	chr19:43684499-43684748	NONHSAT066587
4	lnc-PSG4-1	chr19:43710321-43711451	NONHSAT066590
5	lnc-PSG5-1	chr19:43696890-43697540	NONHSAT066588
6	lnc-PSG9-2	chr19:43762354-43762608	NONHSAT066592
7	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066592
8	lnc-CD177-1	chr19:43658863-43659311	ENSG00000227606.1
9	lnc-CD177-1	chr19:43657665-43657763	ENSG00000227606.1
10	lnc-PSG9-2	chr19:43728324-43728464	NONHSAT066591
11	lnc-AC005392.1-2	chr19:43833447-43833660	ENSG00000231412.2
12	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
13	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066593
14	lnc-PSG5-1	chr19:43699147-43699301	NONHSAT066589
15	lnc-CD177-1	chr19:43665002-43665014	ENSG00000227606.1
16	lnc-PSG9-2	chr19:43763009-43764898	NONHSAT066592
17	lnc-PSG9-1	chr19:43807323-43807688	NONHSAT066594
18	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
19	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066591
20	lnc-PSG9-1	chr19:43808621-43808675	NONHSAT066594
21	lnc-PSG5-1	chr19:43698107-43698746	NONHSAT066589
22	lnc-PSG9-2	chr19:43719405-43719531	NONHSAT066591
23	lnc-PSG4-3	chr19:43672274-43672355	NONHSAT066586
24	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
25	lnc-CD177-3	chr19:43831344-43831587	expReg_chr19_6043_+
26	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
27	lnc-AC005392.1-2	chr19:43835496-43835582	ENSG00000231412.2
28	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
29	lnc-PSG9-2	chr19:43724783-43725023	NONHSAT066593
30	lnc-PSG4-3	chr19:43674207-43674723	NONHSAT066585
31	lnc-PSG9-2	chr19:43752160-43752275	NONHSAT066591
32	lnc-PSG4-3	chr19:43674207-43674717	NONHSAT066586
33	lnc-PSG9-2	chr19:43737376-43737446	NONHSAT066591
34	lnc-PSG9-2	chr19:43752643-43752798	NONHSAT066591
35	lnc-CD177-1	chr19:43659324-43659477	ENSG00000227606.1
36	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591

No data

Variant related genes	Relation type
ENSG00000231412	TF binding region
PSG5	TF binding region
CEACAMP4	TF binding region
CEACAMP10	TF binding region
PSG9	TF binding region
PSG4	TF binding region
CEACAMP11	TF binding region
ENSG00000227606	TF binding region
ENSG00000231412	CpG island
PSG5	CpG island
CEACAMP4	CpG island
CEACAMP10	CpG island
PSG9	CpG island
PSG4	CpG island
CEACAMP11	CpG island
ENSG00000227606	CpG island
ENSG00000243137	chromatin interactions
ENSG00000231412	chromatin interactions

Extended variants
information (count: 9017 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:9017 , 50 per page) page: 1 2 3 4 5 6 7 ... 181

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11667152	chr19:43652661-43652662	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184764021	chr19:43652688-43652689	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs113378986	chr19:43652694-43652695	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs111771916	chr19:43652708-43652709	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs568032052	chr19:43652725-43652726	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs371409854	chr19:43652750-43652751	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs547220330	chr19:43652759-43652760	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs565775193	chr19:43652760-43652761	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs534748635	chr19:43652762-43652763	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs554585895	chr19:43652785-43652786	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs574375499	chr19:43652816-43652817	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs11671801	chr19:43652820-43652821	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs535561667	chr19:43652821-43652822	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs537071967	chr19:43652831-43652832	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs553302970	chr19:43652840-43652841	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs189486573	chr19:43652863-43652864	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs182089353	chr19:43652864-43652865	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs374661042	chr19:43652892-43652893	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs565343921	chr19:43652912-43652913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34910977	chr19:43652931-43652932	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs143706902	chr19:43652939-43652940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572987265	chr19:43652960-43652961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541948969	chr19:43652961-43652962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185280882	chr19:43652969-43652970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530780261	chr19:43652991-43652992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550964863	chr19:43652997-43652998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371063380	chr19:43653053-43653054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558076638	chr19:43653123-43653124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564579221	chr19:43653139-43653140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576556530	chr19:43653182-43653183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111751870	chr19:43653188-43653189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146317590	chr19:43653198-43653199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375231192	chr19:43653219-43653220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543688347	chr19:43653261-43653262	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs189598222	chr19:43653262-43653263	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs7254968	chr19:43653358-43653359	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs144182992	chr19:43653386-43653387	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs140764700	chr19:43653408-43653409	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs568163432	chr19:43653421-43653422	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs536601182	chr19:43653434-43653435	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556918090	chr19:43653436-43653437	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs577054100	chr19:43653469-43653470	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs372063648	chr19:43653498-43653499	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs145126557	chr19:43653533-43653534	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs574004592	chr19:43653534-43653535	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs181202047	chr19:43653535-43653536	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs186654176	chr19:43653539-43653540	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs149105344	chr19:43653566-43653567	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs191416195	chr19:43653598-43653599	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs182895156	chr19:43653600-43653601	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21509527	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21240255	CNVD
Lung squamous cell carcinoma	22363434	CNVD

Chromatin state (count:682 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43650800-43654600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr19:43650800-43655400	Enhancers	NHEK	skin
3	chr19:43651400-43654400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr19:43651600-43654400	Enhancers	HMEC	breast
5	chr19:43651800-43652800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr19:43651800-43653000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr19:43651800-43653800	Enhancers	NHDF-Ad	bronchial
8	chr19:43652000-43653000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr19:43652200-43653200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr19:43652200-43653200	Enhancers	Osteobl	bone
11	chr19:43652200-43655200	Weak transcription	Esophagus	oesophagus
12	chr19:43652400-43652800	Enhancers	Placenta Amnion	Placenta Amnion
13	chr19:43652600-43654400	Enhancers	NHLF	lung
14	chr19:43652800-43653600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr19:43653000-43654000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr19:43653200-43654200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr19:43653200-43656400	Weak transcription	Osteobl	bone
18	chr19:43653600-43654200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr19:43653600-43654400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr19:43653800-43654200	Enhancers	Brain Cingulate Gyrus	brain
21	chr19:43653800-43654200	Weak transcription	NHDF-Ad	bronchial
22	chr19:43654000-43655000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr19:43654200-43654400	Enhancers	Muscle Satellite Cultured Cells	--
24	chr19:43654200-43654400	Enhancers	NHDF-Ad	bronchial
25	chr19:43654400-43656000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr19:43654400-43668200	Weak transcription	NHDF-Ad	bronchial
27	chr19:43654600-43655000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr19:43655000-43655400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr19:43655000-43655600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr19:43655200-43655600	Enhancers	Esophagus	oesophagus
31	chr19:43655400-43655600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr19:43655600-43656600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr19:43655600-43656800	Weak transcription	Esophagus	oesophagus
34	chr19:43655600-43665200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr19:43656000-43657000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr19:43656400-43656800	Enhancers	Osteobl	bone
37	chr19:43656600-43657000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr19:43657000-43657200	Enhancers	Esophagus	oesophagus
39	chr19:43662600-43663600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr19:43662800-43663200	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr19:43662800-43663400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr19:43662800-43663400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr19:43662800-43663600	Enhancers	A549	lung
44	chr19:43663000-43663600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr19:43663000-43663600	Enhancers	NHEK	skin
46	chr19:43663200-43663400	Enhancers	HSMMtube	muscle
47	chr19:43663200-43663600	Enhancers	HMEC	breast
48	chr19:43663600-43666000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr19:43663600-43666000	Weak transcription	HMEC	breast
50	chr19:43663600-43666000	Weak transcription	NHEK	skin

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